Variant report

Variant	nsv999102
Chromosome Location	chr4:9633247-9794181
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1738)
CpG islands
(count:2016)
Chromatin interactive
region (count:37)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1738 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:9705188-9705304	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:9764889-9764976	K562	blood:	n/a	n/a
3	ATF1	chr4:9693437-9693703	K562	blood:	n/a	n/a
4	ATF1	chr4:9758253-9758343	K562	blood:	n/a	n/a
5	ATF2	chr4:9764713-9765001	GM12878	blood:	n/a	n/a
6	BACH1	chr4:9689846-9689882	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:9784048-9784153	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr4:9661312-9661676	GM12878	blood:	n/a	n/a
9	BATF	chr4:9709684-9709950	GM12878	blood:	n/a	n/a
10	BATF	chr4:9637521-9637725	GM12878	blood:	n/a	n/a
11	BATF	chr4:9709608-9710002	GM12878	blood:	n/a	n/a
12	BATF	chr4:9697635-9697868	GM12878	blood:	n/a	n/a
13	BATF	chr4:9715614-9715953	GM12878	blood:	n/a	n/a
14	BATF	chr4:9779146-9779367	GM12878	blood:	n/a	n/a
15	BATF	chr4:9661377-9661663	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:9709736-9710003	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:9779122-9779297	GM12878	blood:	n/a	n/a
18	BCL11A	chr4:9709714-9709970	GM12878	blood:	n/a	n/a
19	BCL11A	chr4:9661303-9661712	GM12878	blood:	n/a	n/a
20	BCL11A	chr4:9637557-9637806	GM12878	blood:	n/a	n/a
21	BCL11A	chr4:9693955-9694191	GM12878	blood:	n/a	n/a
22	BCL3	chr4:9747374-9747670	GM12878	blood:	n/a	n/a
23	BCL3	chr4:9747263-9747923	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:9693347-9693648	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:9764726-9765039	K562	blood:	n/a	n/a
26	BHLHE40	chr4:9764795-9765105	HepG2	liver:	n/a	n/a
27	BHLHE40	chr4:9693135-9693538	HepG2	liver:	n/a	chr4:9693155-9693171
28	BHLHE40	chr4:9733756-9733953	K562	blood:	n/a	n/a
29	BHLHE40	chr4:9697620-9697865	HepG2	liver:	n/a	n/a
30	BHLHE40	chr4:9705121-9705321	K562	blood:	n/a	n/a
31	BHLHE40	chr4:9705080-9705313	GM12878	blood:	n/a	n/a
32	BHLHE40	chr4:9764736-9765042	GM12878	blood:	n/a	n/a
33	BHLHE40	chr4:9661297-9661608	HepG2	liver:	n/a	n/a
34	BHLHE40	chr4:9693184-9693740	K562	blood:	n/a	n/a
35	CBX3	chr4:9709655-9709945	K562	blood:	n/a	n/a
36	CCNT2	chr4:9693190-9693570	K562	blood:	n/a	n/a
37	CEBPB	chr4:9766267-9766705	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:9720182-9720485	K562	blood:	n/a	chr4:9720327-9720338
39	CEBPB	chr4:9725682-9725793	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:9759045-9759325	A549	lung:	n/a	n/a
41	CEBPB	chr4:9759126-9759326	IMR90	lung:	n/a	n/a
42	CEBPB	chr4:9637488-9637693	HepG2	liver:	n/a	chr4:9637617-9637628
43	CEBPB	chr4:9764821-9764973	K562	blood:	n/a	n/a
44	CEBPB	chr4:9720234-9720515	HepG2	liver:	n/a	chr4:9720327-9720338
45	CEBPB	chr4:9759118-9759224	K562	blood:	n/a	n/a
46	CEBPB	chr4:9661262-9661447	K562	blood:	n/a	n/a
47	CEBPB	chr4:9639784-9639891	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr4:9765383-9765597	HepG2	liver:	n/a	chr4:9765508-9765519
49	CEBPB	chr4:9727679-9727879	HepG2	liver:	n/a	chr4:9727792-9727803 chr4:9727792-9727805
50	CEBPD	chr4:9712816-9713034	K562	blood:	n/a	n/a

(count:2016 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9783192-9783242	SAEC	small airway:	n/a
2	chr4:9760275-9760325	IMR90	lung:	fetal
3	chr4:9693516-9693566	AG04449	skin:	fetal
4	chr4:9783192-9783242	SAEC	small airway:	n/a
5	chr4:9760275-9760325	IMR90	lung:	fetal
6	chr4:9693516-9693566	AG04449	skin:	fetal
7	chr4:9661422-9661472	LNCaP	prostate:	n/a
8	chr4:9783196-9783246	Caco-2	colon:	n/a
9	chr4:9709042-9709092	SK-N-MC	brain:	n/a
10	chr4:9653008-9653058	AG04449	skin:	fetal
11	chr4:9696916-9696966	HPAEpiC	pulmonary alveolar:	n/a
12	chr4:9760736-9760786	MCF10A-Er-Src	breast:	n/a
13	chr4:9709042-9709092	AG09319	gingival:	n/a
14	chr4:9760275-9760325	ovcar-3	ovarian:	n/a
15	chr4:9661422-9661472	HNPCEpiC	eye:	n/a
16	chr4:9783953-9784003	HCM	heart:	n/a
17	chr4:9783363-9783413	HL-60	blood:	n/a
18	chr4:9760275-9760325	Caco-2	colon:	n/a
19	chr4:9783398-9783448	NT2-D1	testis:	n/a
20	chr4:9783198-9783248	GM12878	blood:	n/a
21	chr4:9783623-9783673	HCM	heart:	n/a
22	chr4:9783953-9784003	NHBE	bronchial:	n/a
23	chr4:9783363-9783413	AG09309	skin:	n/a
24	chr4:9782243-9782293	NHDF-neo	bronchial:	n/a
25	chr4:9693329-9693379	NH-A	brain:	n/a
26	chr4:9784508-9784558	HNPCEpiC	eye:	n/a
27	chr4:9783196-9783246	NHDF-neo	bronchial:	n/a
28	chr4:9762166-9762216	BJ	skin:	n/a
29	chr4:9693764-9693814	GM19239	blood:	n/a
30	chr4:9693764-9693814	AoSMC	blood vessel:	n/a
31	chr4:9783965-9784015	NHBE	bronchial:	n/a
32	chr4:9696916-9696966	AG09319	gingival:	n/a
33	chr4:9762166-9762216	ECC-1	luminal epithelium:	n/a
34	chr4:9696916-9696966	HAEpiC	amniotic membrane:	n/a
35	chr4:9693516-9693566	HCM	heart:	n/a
36	chr4:9762166-9762216	H1-hESC	embryonic stem cell:	embryo
37	chr4:9661422-9661472	SK-N-SH_RA	brain:	n/a
38	chr4:9689364-9689414	GM12892	blood:	n/a
39	chr4:9783623-9783673	Caco-2	colon:	n/a
40	chr4:9760736-9760786	HMEC	breast:	n/a
41	chr4:9782891-9782941	AG09319	gingival:	n/a
42	chr4:9783198-9783248	Hepatocyte	liver:	n/a
43	chr4:9692836-9692886	Hepatocyte	liver:	n/a
44	chr4:9783363-9783413	HMEC	breast:	n/a
45	chr4:9693516-9693566	A549	lung:	n/a
46	chr4:9696916-9696966	GM12891	blood:	n/a
47	chr4:9692836-9692886	GM06990	blood:	n/a
48	chr4:9787734-9787784	H1-hESC	embryonic stem cell:	embryo
49	chr4:9783965-9784015	Hela-S3	cervix:	n/a
50	chr4:9661422-9661472	PANC-1	pancreas:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:9764792..9765537-chr4:9899989..9900954,5	MCF-7	breast:
2	chr2:91818675..91820415-chr4:9765033..9768552,3	K562	blood:
3	chr1:149221736..149225365-chr4:9763717..9766826,4	MCF-7	breast:
4	chr4:9705013..9706114-chr4:10020117..10020881,3	MCF-7	breast:
5	chr4:9766485..9767197-chr4:10016698..10017481,2	MCF-7	breast:
6	chr4:9699934..9701585-chr4:10019007..10021805,2	K562	blood:
7	chr4:9704779..9705714-chr4:10015117..10016069,5	MCF-7	breast:
8	chr4:9761130..9763005-chr4:9988480..9990175,2	K562	blood:
9	chr4:9764793..9765717-chr4:10015113..10016017,3	MCF-7	breast:
10	chr4:9766848..9767385-chr4:9900038..9900893,4	MCF-7	breast:
11	chr2:91815162..91820044-chr4:9763391..9768700,25	MCF-7	breast:
12	chr4:9705037..9705657-chr4:9778184..9778690,2	K562	blood:
13	chr2:91817635..91819182-chr4:9766044..9767255,9	MCF-7	breast:
14	chr4:9766486..9767204-chr4:10064960..10065893,2	MCF-7	breast:
15	chr4:9533415..9534346-chr4:9660887..9661684,2	MCF-7	breast:
16	chr4:9764370..9765339-chr4:10015197..10016013,4	MCF-7	breast:
17	chr4:9764866..9765415-chr4:9928949..9929492,2	MCF-7	breast:
18	chr1:149220703..149225113-chr4:9764948..9767069,4	MCF-7	breast:
19	chr4:9770192..9773137-chr4:10024212..10026749,2	K562	blood:
20	chr2:91818363..91818948-chr4:9766445..9767270,6	MCF-7	breast:
21	chr4:9764437..9765430-chr4:10020023..10020916,6	MCF-7	breast:
22	chr4:9704873..9705750-chr4:10016280..10017221,3	K562	blood:
23	chr2:91818108..91819097-chr4:9766527..9767180,2	K562	blood:
24	chr4:9764445..9765327-chr4:10020033..10020988,3	K562	blood:
25	chr4:9766550..9767471-chr4:10020110..10020837,2	MCF-7	breast:
26	chr4:9764417..9765133-chr4:10016121..10017439,5	MCF-7	breast:
27	chr2:91816088..91820118-chr4:9765029..9767622,10	MCF-7	breast:
28	chr2:91816443..91817305-chr4:9764390..9765414,6	MCF-7	breast:
29	chr2:91816303..91817383-chr4:9764391..9765414,6	MCF-7	breast:
30	chr4:9765483..9767943-chr4:10007316..10009788,2	MCF-7	breast:
31	chr4:9705037..9705657-chr4:9778184..9778690,2	K562	blood:
32	chr4:9766226..9767390-chr4:9899951..9901032,8	MCF-7	breast:
33	chr4:9764428..9765300-chr4:10016550..10017565,3	K562	blood:
34	chr2:91815622..91818416-chr4:9765055..9766802,2	K562	blood:
35	chr4:9763456..9766236-chr4:10014004..10016919,3	K562	blood:
36	chr2:91815178..91817122-chr4:9765055..9766792,2	K562	blood:
37	chr2:91816400..91817015-chr4:9766701..9767270,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC2A9-1	chr4:9686325-9686330	XLOC_003881
2	lnc-DRD5-15	chr4:9681973-9682135	l_2602_chr4:9680111-9682135_thyroid
3	lnc-SLC2A9-2	chr4:9693361-9693365	XLOC_003880
4	lnc-DRD5-15	chr4:9680112-9680551	l_2602_chr4:9680111-9682135_thyroid
5	lnc-SLC2A9-2	chr4:9682416-9682671	XLOC_003880
6	lnc-SLC2A9-1	chr4:9691882-9692319	XLOC_003881
7	lnc-SLC2A9-6	chr4:9680180-9680546	l_2603_chr4:9680179-9682164_kidney
8	lnc-DRD5-16	chr4:9678932-9679558	NONHSAT095141
9	lnc-SLC2A9-6	chr4:9681968-9682164	l_2603_chr4:9680179-9682164_kidney

No data

Variant related genes	Relation type
FAM86MP	TF binding region
ENSG00000249563	TF binding region
ALG1L3P	TF binding region
DRD5	TF binding region
ENPP7P11	TF binding region
OR7E35P	TF binding region
FAM86MP	CpG island
ENSG00000249563	CpG island
ALG1L3P	CpG island
DRD5	CpG island
ENPP7P11	CpG island
OR7E35P	CpG island
ENSG00000206737	chromatin interactions
ENSG00000250413	chromatin interactions
ENSG00000109667	chromatin interactions
FBXW7	miRNA target sites

Extended variants
information (count: 9589 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:9589 , 50 per page) page: 1 2 3 4 5 6 7 ... 192

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556619520	chr4:9633262-9633263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370456725	chr4:9633277-9633278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563863877	chr4:9633286-9633287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531281312	chr4:9633321-9633322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs573090330	chr4:9633327-9633328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188056305	chr4:9633330-9633331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148858193	chr4:9633357-9633358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533967988	chr4:9633366-9633367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371170513	chr4:9633369-9633370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568179591	chr4:9633381-9633382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191253456	chr4:9633387-9633388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373629129	chr4:9633406-9633407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs9291589	chr4:9633410-9633411	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs568710653	chr4:9633418-9633419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184826225	chr4:9633421-9633422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs117930056	chr4:9633432-9633433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577196657	chr4:9633434-9633435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535039613	chr4:9633438-9633439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553058293	chr4:9633447-9633448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372032779	chr4:9633454-9633455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs62410035	chr4:9633505-9633506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs62410036	chr4:9633510-9633511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs62410037	chr4:9633513-9633514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs62410038	chr4:9633514-9633515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527338187	chr4:9633524-9633525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs6831137	chr4:9633547-9633548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541911629	chr4:9633549-9633550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs77118731	chr4:9633558-9633559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575895160	chr4:9633576-9633577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs546552180	chr4:9633579-9633580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187690784	chr4:9633629-9633630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368337050	chr4:9633642-9633643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528749519	chr4:9633669-9633670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563348103	chr4:9633680-9633681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540236149	chr4:9633685-9633686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192197026	chr4:9633688-9633689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147992205	chr4:9633689-9633690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559970263	chr4:9633696-9633697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs6836184	chr4:9633711-9633712	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs185109418	chr4:9633724-9633725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs6836196	chr4:9633728-9633729	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs566774316	chr4:9633741-9633742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533804574	chr4:9633744-9633745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553335132	chr4:9633749-9633750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189571652	chr4:9633765-9633766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181588428	chr4:9633768-9633769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557473354	chr4:9633783-9633784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141628047	chr4:9633784-9633785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184700701	chr4:9633820-9633821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558032185	chr4:9633821-9633822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Sinonasal adenocarcinoma	21360264	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:653 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9624800-9637600	Weak transcription	Brain Hippocampus Middle	brain
2	chr4:9627000-9639000	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr4:9627800-9634400	Weak transcription	Brain Anterior Caudate	brain
4	chr4:9634400-9639400	Enhancers	Fetal Thymus	thymus
5	chr4:9637800-9638800	Enhancers	Thymus	Thymus
6	chr4:9640800-9643000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr4:9643000-9643800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr4:9643200-9645800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr4:9643800-9644000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr4:9661200-9661400	Enhancers	Fetal Muscle Leg	muscle
11	chr4:9661200-9662200	Weak transcription	Fetal Thymus	thymus
12	chr4:9661400-9662600	Weak transcription	Fetal Muscle Leg	muscle
13	chr4:9662600-9662800	Enhancers	Fetal Muscle Leg	muscle
14	chr4:9662800-9663400	Weak transcription	Fetal Muscle Leg	muscle
15	chr4:9663400-9663600	Enhancers	Fetal Muscle Leg	muscle
16	chr4:9664800-9675600	Weak transcription	Fetal Thymus	thymus
17	chr4:9672400-9672600	Enhancers	Brain Hippocampus Middle	brain
18	chr4:9672400-9672600	Enhancers	Fetal Stomach	stomach
19	chr4:9672400-9672600	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr4:9672400-9672800	Enhancers	Ovary	ovary
21	chr4:9672400-9673000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr4:9672400-9673000	Enhancers	Fetal Lung	lung
23	chr4:9672400-9673000	Enhancers	Left Ventricle	heart
24	chr4:9672400-9673000	Enhancers	Right Atrium	heart
25	chr4:9672400-9673200	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr4:9672400-9673200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr4:9672400-9687000	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr4:9672600-9673000	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr4:9672600-9673000	Enhancers	Fetal Muscle Trunk	muscle
30	chr4:9672600-9673000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
31	chr4:9672600-9673200	Enhancers	Fetal Muscle Leg	muscle
32	chr4:9673000-9692400	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr4:9673200-9692600	Weak transcription	Fetal Muscle Leg	muscle
34	chr4:9675600-9676000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr4:9675600-9676000	Enhancers	Fetal Thymus	thymus
36	chr4:9675600-9676200	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr4:9676600-9680000	Weak transcription	Brain Anterior Caudate	brain
38	chr4:9676600-9681200	Weak transcription	Fetal Stomach	stomach
39	chr4:9680200-9680800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr4:9681200-9682000	ZNF genes & repeats	Fetal Stomach	stomach
41	chr4:9681400-9681600	Weak transcription	Fetal Thymus	thymus
42	chr4:9681600-9682000	ZNF genes & repeats	Fetal Thymus	thymus
43	chr4:9682000-9683000	Weak transcription	Fetal Stomach	stomach
44	chr4:9682000-9686800	Weak transcription	Fetal Thymus	thymus
45	chr4:9686800-9687200	Enhancers	Brain Germinal Matrix	brain
46	chr4:9686800-9687200	Enhancers	Fetal Thymus	thymus
47	chr4:9686800-9687800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr4:9687000-9687600	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr4:9687000-9687600	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr4:9687200-9691800	Weak transcription	Fetal Thymus	thymus

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